5660-61-7

Basic information

• Product Name: 2-(3-oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)-N-[2-(trifluoromethyl)phenyl]acetamide
• Synonyms: 2-(3-Oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)-N-[2-(trifluoromethyl)phenyl]acetamide; 2-quinoxalineacetamide, 1,2,3,4-tetrahydro-3-oxo-N-[2-(trifluoromethyl)phenyl]-
• CAS NO: 5660-61-7
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 349.3072
• Mol File: 5660-61-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 591.7°C at 760 mmHg
• Flash Point: 311.6°C
• Density: 1.359g/cm³
• Vapor Pressure: 5.66E-14mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: 2-(3-oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)-N-[2-(trifluoromethyl)phenyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)-N-[2-(trifluoromethyl)phenyl]acetamide(5660-61-7)
• EPA Substance Registry System: 2-(3-oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)-N-[2-(trifluoromethyl)phenyl]acetamide(5660-61-7)

Safety Data

• Hazardous Substances Data: 5660-61-7(Hazardous Substances Data)

Upstream product

• 513-85-9 2.3-butanediol 
• 17226-65-2 (R,S)-2,2,4,5-tetramethyl-1,3-dioxolane 
• 67-64-1 acetone 
• 925669-95-0 2,3-cis-epoxybutane 
• 6982-25-8 d,l-2,3-butanediol 

Downstream Products

• 5798-81-2 2-acetoxy-3-bromobutane 
• 67-64-1 acetone 
• 17226-65-2 (R,S)-2,2,4,5-tetramethyl-1,3-dioxolane 

Relevant articles and documents

Catalytic conversion of epoxides to 1,3-dioxolanes with phosphomolybdic acid (PMA) in solution and under solvent-free conditions

The fast and efficient conversion of epoxides into 2,2-dimethyl-1,3- dioxolanes was studied with catalytic amounts of phosphomolybdic acid (PMA) (0.1-0.2 mol %) at room temperature in solution and under solvent-free conditions. The products were obtained in high to excellent yields within 1-2 min. Copyright Taylor & Francis Group, LLC.

Aerobic Oxidation of Vicinal Diols Catalyzed by an Anderson-Type Polyoxometalate, [IMo6O24]5-

An Anderson-type polyoxometalate, [IVIIMo6O24]5-, has been used as a catalyst for the aerobic oxidation at 80°C of vicinal diols (glycols). This is the first report on the use of such a polyoxometalate as an oxi

Synthesis of 1,3-dioxolanes by the addition of ketones to epoxides by using [Cp*Ir(NCMe)3]2+ as catalyst

A series of 1,3-dioxolanes have been prepared by the addition of ketones to epoxides in the presence of the catalyst [Cp*Ir(NCMe)3]2+, Cp=C5Me5. The reactions proceed readily at 22°C and the yields are good. The following 1,3-dioxolanes: 2,2,4-trimethyl-1,3-dioxolane, 1; 2,2-dimethyl-4-vinyl-1,3-dioxolane, 2; 2,2-dimethyl-4-phenyl-1,3-dioxolane, 3; 2,2-diethyl-4-methyl-1,3-dioxolane, 4; 2,2-diethyl-4-vinyl-1,3-dioxolane, 5; 2,2-diethyl-4-phenyl-1,3-dioxolane, 6 were prepared from the appropriate epoxide and carbonyl compounds. An inversion of configuration at the carbon atom at the C-O bond cleavage site of the epoxide was observed to occur in the formation of the dioxolanes: R, S,- 2,2,4,5-tetramethyl-1,3-dioxolane, 7 and a mixture of R,R- and S,S-2,2,4,5-tetramethyl-1,3-dioxolane, 8 obtained from the reactions of acetone with R, R,-/S, S,-buten-2-oxide and R, S,-buten-2-oxide, respectively.